United States · FDA National Drug Code directory
HYDROMORPHONE HYDROCHLORIDE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63629-2532_971f9f4c-1e16-40fb-b08f-e5dc1424e2d2
- Product NDC
- 63629-2532
- Form
- SUPPOSITORY
- Composition / generic term
- HYDROMORPHONE HYDROCHLORIDE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 19960131
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROMORPHONE HYDROCHLORIDE — 3 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 PACKET in 1 BOX (63629-2532-1) / 1 SUPPOSITORY in 1 PACKET · 63629-2532-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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